eudamed_udi
Primary ID: 08684887760091
AlpCe (UDI 08684887760091)
Manufactured by ALPCE MEDİKAL SAN.VE TİC.LTD.ŞTİ
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AlpCe - Primary ID 08684887760091
Device Regulatory Overview
The AlpCe (Model/Catalog Number: ACM-ERK200DB) is a medical device manufactured by ALPCE MEDİKAL SAN.VE TİC.LTD.ŞTİ. This product is indexed under FDA Product Code / Category Classification V08060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACM-ERK200DB
- Product Code / EMDN
- V08060101
- Device Name
- PATIENT BED WITH DUAL MOTOR AND WOODEN HEAD BOARDS
- Database Sync Date
- 2026-08-09 16:47:32
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of AlpCe?
The registered manufacturer of record for AlpCe is ALPCE MEDİKAL SAN.VE TİC.LTD.ŞTİ.
What is the Primary UDI-DI identifier for AlpCe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684887760091.
What classification code is assigned to this device?
This device is registered under product classification code V08060101.
Similar Classification Devices (V08060101)
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